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Hereditary angioedema with C1 inhibitor deficiency: delay in diagnosis in Europe
BACKGROUND: Hereditary angioedema (HAE) is a rare, debilitating, and potentially life-threatening disease characterized by recurrent edema attacks. Important advances in HAE treatment have been made, including the development of new therapies for treating or preventing attacks. Nevertheless, the dis...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3751114/ https://ncbi.nlm.nih.gov/pubmed/23937903 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1710-1492-9-29 |
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